## Abstract The identification and complete ^13^C and ^1^H assignment of a sample of oligomycin A is described. ^13^C multiplicities were determined by the INEPT method; assignments were made by comparison of heteronuclear ^13^C‐^1^H chemical shift correlation, homonuclear COSY and homonuclear rela
Identification and ab initio carbon-13 NMR assignment of a proanthocyanidin from Prunus jacquemontii
✍ Scribed by Geeta Pant; Anil K. Nautiyal; Mohan S. M. Rawat; James K. Sutherland; Gareth A. Morris
- Book ID
- 102525804
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 403 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The concerted use of 1D and 2D multiple pulse NMR methods allowed the identification and assignment of a proanthocyanidin, ent‐epiafzelechin(4α → 8; 2α → O → 7)‐epicatechin, extracted from the bark of Prunus jacquemontii. Reference deconvolution with the FIDDLE algorithm was successfully used for line shape correction of a ^13^C spectrum with poor signal‐to‐noise ratio. Over 70 long‐range proton– ^13^C correlations were determined with the HMBC experiment, following modifications to improve instrument signal reproducibility, illustrating the value of this experiment when applied to systems with relatively few protons.
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